In vitro transdermal delivery of the major catechins and caffeine from extract of Camellia sinensis.

Abstract:

:The aim of this study was to investigate the feasibility of the transdermal delivery of catechins and caffeine from green tea extract. Drug-in-adhesive patches containing 1.35, 1.03, 0.68, and 0.32 mg cm(-2) green tea extract were formulated and the dissolution of (-)-epigallocatechin gallate (EGCg), (-)-epigallocatechin (EGC) and (-)-epicatechin (EC) from these was determined. Transdermal delivery was determined across full thickness pig ear skin from saturated solutions of green tea extract in pH 5.5 citrate-phosphate buffer, polyethylene glycol 400 and a 50:50 mixture of the citrate phosphate buffer and polyethylene glycol in addition to patches containing 1.35 mg cm(-2) green tea extract. Dissolution experiments indicated first order release which was dose dependent in respect of the loading level, although the amounts permeated were not always proportional to the amounts in the formulation. The highest percentage permeation of EGCg was found to be from the patch formulation. EGCg, EGC and EC were all successfully delivered transdermally from saturated solutions and adhesive patches containing green tea extract in this study. There was some evidence for the dermal metabolism of EGCg, but after 24 h 0.1% permeated from the patches containing 1.35 mg cm(-2) green tea extract. This was equivalent to the percentage absorbed after intragastric administration of green tea extract in rats. In addition, the concentration of EGCg in the Franz cell receptor chamber after 24 h permeation from the 0.9 cm diameter patch containing 1.35 mg cm(-2) was within the range of Cmax plasma levels achieved after oral dosing of 2.2-4.2 gm(-2) green tea extract. Caffeine was also delivered at concentrations above those previously reported.

journal_name

Int J Pharm

authors

Batchelder RJ,Calder RJ,Thomas CP,Heard CM

doi

10.1016/j.ijpharm.2004.06.007

keywords:

subject

Has Abstract

pub_date

2004-09-28 00:00:00

pages

45-51

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378517304003436

journal_volume

283

pub_type

杂志文章
  • Understanding die fill variation during mini-tablet production.

    abstract::Reproducibility of die fill during tablet production is critical to ensure consistent tablet drug content and mechanical attributes. In the production of mini-tablets, tablets smaller than 6mm, achievement of uniform die fill is much more challenging. Powder flow is often associated with die fill accuracy but this rel...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.10.042

    authors: Goh HP,Heng PWS,Liew CV

    更新日期:2017-12-20 00:00:00

  • Localized drug delivery with mono and bilayered mucoadhesive films and wafers for oral mucosal infections.

    abstract::Local drug delivery into oral cavity offers many advantages over systemic administration in treatment of the oral infections. In this study, monolayer and bilayered mucoadhesive film and wafer formulations were developed as local drug delivery platforms using chitosan and hydroxypropyl methylcellulose (HPMC). Cefuroxi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.01.029

    authors: Timur SS,Yüksel S,Akca G,Şenel S

    更新日期:2019-03-25 00:00:00

  • Preparation of nimodipine-loaded microemulsion for intranasal delivery and evaluation on the targeting efficiency to the brain.

    abstract::The purpose of this study was to improve the solubility and enhance the brain uptake of nimodipine (NM) in an o/w microemulsion, which was suitable for intranasal delivery. Three microemulsion systems stabilized by the nonionic surfactants either Cremophor RH 40 or Labrasol, and containing a variety of oils, namely is...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.01.039

    authors: Zhang Q,Jiang X,Jiang W,Lu W,Su L,Shi Z

    更新日期:2004-05-04 00:00:00

  • Skin penetration and deposition of carboxyfluorescein and temoporfin from different lipid vesicular systems: In vitro study with finite and infinite dosage application.

    abstract::The aim of the present research is to evaluate the influence of different lipid vesicular systems as well as the effect of application mode on skin penetration and deposition behaviors of carboxyfluorescein (hydrophilic model drug) and temoporfin (lipophilic model drug). All of the lipid vesicular systems, including c...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.02.006

    authors: Chen M,Liu X,Fahr A

    更新日期:2011-04-15 00:00:00

  • Dehydration behavior of nedocromil magnesium pentahydrate.

    abstract::The dehydration of nedocromil magnesium (NM) pentahydrate proceeds in two steps, corresponding to the loss of four water molecules in the first step and one water molecule in the second step. The effects of temperature, particle size, sample weight, water vapor pressure and dehydration-rehydration cycle on both the ki...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00700-6

    authors: Zhu H,Grant DJ

    更新日期:2001-03-14 00:00:00

  • Mucoadhesive microspheres prepared by interpolymer complexation and solvent diffusion method.

    abstract::Mucoadhesive microspheres were prepared to increase gastric residence time using an interpolymer complexation of poly(acrylic acid) (PAA) with poly(vinyl pyrrolidone) (PVP) and a solvent diffusion method. The complexation between poly(acrylic acid) and poly(vinyl pyrrolidone) as a result of hydrogen bonding was confir...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.10.016

    authors: Chun MK,Cho CS,Choi HK

    更新日期:2005-01-20 00:00:00

  • Chitosan/cyclodextrin nanoparticles as macromolecular drug delivery system.

    abstract::The aim of this study was to generate a new type of nanoparticles made of chitosan (CS) and carboxymethyl-beta-cyclodextrin (CM-beta-CD) and to evaluate their potential for the association and delivery of macromolecular drugs. CS and CM-beta-CD or mixtures of CM-beta-CD/tripolyphosphate (TPP) were processed to nanopar...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.03.005

    authors: Krauland AH,Alonso MJ

    更新日期:2007-08-01 00:00:00

  • Comparison of the IV pharmacokinetics in sheep of miconazole-cyclodextrin solutions and a micellar solution.

    abstract::The pharmacokinetics of miconazole were studied after intravenous administration to six sheep (4 mg/kg) of three aqueous solutions: a marketed micellar solution containing polyoxyl-35 castor oil (Daktarin IV(R)) was compared with two solutions both containing 50 mM lactic acid and a cyclodextrin derivative (100 mM HP-...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(98)00403-7

    authors: Piel G,Evrard B,Van Hees T,Delattre L

    更新日期:1999-03-25 00:00:00

  • Innovative pMDI formulations of spray-dried nanoparticles for efficient pulmonary drug delivery.

    abstract::For drug delivery to the lungs, the aerodynamic size of drug particles plays a predominant role in determining the sites of deposition in the airway, and the particles with the size less than 2μm are highly expected as they will be preferably delivered to the ideal site of alveolar regions. In this paper, a novel plat...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.07.040

    authors: Li HY,Xu EY

    更新日期:2017-09-15 00:00:00

  • Suppression of agglomeration in fluidized bed coating. II. Measurement of mist size in a fluidized bed chamber and effect of sodium chloride addition on mist size.

    abstract::It has been reported that the degree of particle agglomeration in fluidized bed coating is greatly affected by the spray mist size of coating solution. However, the mist size has generally been measured in open air, and few reports have described the measurement of the mist size in a chamber of the fluidized bed, in w...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(98)00370-6

    authors: Yuasa H,Nakano T,Kanaya Y

    更新日期:1999-02-01 00:00:00

  • Development of a cyclodextrin-based aqueous cyclosporin A eye drop formulations.

    abstract::Cyclosporin A (CyA) is a lipophilic, cyclic polypeptide drug with anti-inflammatory properties. It is used in topical treatment of dry eyes and is now commercially available in oil based surfactant containing eye drops. Surfactants can irritate the eye surface causing burning, itching and irritation of the conjunctiva...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.07.040

    authors: Jóhannsdóttir S,Jansook P,Stefánsson E,Loftsson T

    更新日期:2015-09-30 00:00:00

  • Designing optimal formulations for hot-melt coating.

    abstract::Hot-melt coating (HMC) as a solvent-free technology grants faster and more economic coating processes with reduced risk of dissolving the drug during the process. Moreover, traditional coating equipment can be modified to enable the HMC process. Despite the indubitable advantages and feasibility of the process, HMC is...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.08.086

    authors: Lopes DG,Salar-Behzadi S,Zimmer A

    更新日期:2017-11-30 00:00:00

  • Ascorbyl-dipalmitate-stabilised nanoemulsions as a potential localised treatment of inflammatory bowel diseases.

    abstract::Current efforts on inflammatory bowel diseases (IBD) treatment are focused on strategies for localised drug delivery at the intestinal mucosa. Despite the potential of curcumin (CC) for IBD treatment, its low solubility and stability limit its application. Thus, the design of nanocarriers that focus CC delivery at the...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119533

    authors: Plaza-Oliver M,Beloqui A,Santander-Ortega MJ,Castro-Vázquez L,Rodríguez-Robledo V,Arroyo-Jiménez MM,Préat V,Lozano MV

    更新日期:2020-08-30 00:00:00

  • The application of STEP-technology® for particle and protein dispersion detection studies in biopharmaceutical research.

    abstract::Particle detection and analysis techniques are essential in biopharmaceutical industries to evaluate the quality of various parenteral formulations regarding product safety, product quality and to meet the regulations set by the authority agencies. Several particle analysis systems are available on the market, but for...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.03.050

    authors: Gross-Rother J,Herrmann N,Blech M,Pinnapireddy SR,Garidel P,Bakowsky U

    更新日期:2018-05-30 00:00:00

  • Establishing and analyzing the design space in the development of direct compression formulations by gene expression programming.

    abstract:PURPOSE:In this paper we have evaluated the gene expression programming (GEP) methodology for modeling the effect of different variables (continuous and nominal) and their interactions on the properties of direct compression formulations. METHODS:The effect of four variables was studied; variety of diluents, type and ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.04.078

    authors: Landin M,Rowe RC,York P

    更新日期:2012-09-15 00:00:00

  • Novel combination of non-invasive morphological and solid-state characterisation of drug-loaded core-shell electrospun fibres.

    abstract::In recent years, core-shell nanofibrous drug delivery systems have received increasing attention due to their ability to incorporate two or more active pharmaceutical ingredients (APIs) individually into the desired layer (either core or sheath) and thereby finely tune the release profiles of even incompatible drugs i...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119706

    authors: Kazsoki A,Farkas A,Balogh-Weiser D,Mancuso E,Sharma PK,Lamprou DA,Zelkó R

    更新日期:2020-09-25 00:00:00

  • Encapsulation of an antivasospastic drug, fasudil, into liposomes, and in vitro stability of the fasudil-loaded liposomes.

    abstract::The objectives of this work were to develop a liposomal fasudil, an antivasospastic drug, as a possible means to deliver the encapsulated drug to the brain, and to characterize the stability of the liposomal formulation in vitro. Transmembrane electrochemical gradients of H+ or ammonium sulfate were created, and their...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00896-1

    authors: Ishida T,Takanashi Y,Doi H,Yamamoto I,Kiwada H

    更新日期:2002-01-31 00:00:00

  • The place of dosage form innovation and the OTC market: the price to pay.

    abstract:AIMS AND OBJECTIVES:The aims and objectives of this article are to provide a background to the innovations that are made in over the counter market and to outline the time and costs involved in these activities. ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.02.042

    authors: Goggin PL

    更新日期:2014-08-05 00:00:00

  • Sustained release ophthalmic dexamethasone: In vitro in vivo correlations derived from the PK-Eye.

    abstract::Corticosteroids have long been used to treat intraocular inflammation by intravitreal injection. We describe dexamethasone loaded poly-DL-lactide-co-glycolide (PLGA) microparticles that were fabricated by thermally induced phase separation (TIPS). The dexamethasone loaded microparticles were evaluated using a two-comp...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.02.047

    authors: Awwad S,Day RM,Khaw PT,Brocchini S,Fadda HM

    更新日期:2017-04-30 00:00:00

  • Enhanced solid-state stability of amorphous ibrutinib formulations prepared by hot-melt extrusion.

    abstract::One of the applications of Hot-Melt Extrusion (HME) is the stabilization of amorphous drugs through its incorporation into polymeric blends in the form of Amorphous Solid Dispersions (ASDs). In this study, HME was applied to solve a real problem in the development of an ibrutinib product, stabilizing the amorphous for...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119156

    authors: Simões MF,Nogueira BA,Tabanez AM,Fausto R,Pinto RMA,Simões S

    更新日期:2020-04-15 00:00:00

  • Evaluation of a ureteral catheter coating by means of a BioEncrustation in vitro model.

    abstract::Biomaterials for applications in the urinary tract are challenged with both biofilm formation and encrustation, two highly interconnected processes. While great effort has been achieved developing promising materials there is only a limited choice of sophisticated in vitro models that are available to analyse the perf...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.04.023

    authors: Frant M,Dayyoub E,Bakowsky U,Liefeith K

    更新日期:2018-07-30 00:00:00

  • Incorporation of benzoyl peroxide nanocrystals into adapalene-loaded solid lipid microparticles: Part II - Solid-in-Oil dispersion of nanoparticulate benzoyl peroxide.

    abstract::Benzoyl peroxide as a monotherapeutic and in combination with adapalene is a cornerstone of current acne therapy, but its unfavourable side effect profile reduces the therapeutic value of this compound. The incorporation into an adapalene-loaded microparticulate lipid matrix, which - via the principle of targeted eros...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118792

    authors: Brammann C,Müller-Goymann CC

    更新日期:2019-12-15 00:00:00

  • Microemulsion-based hydrogel formulation of ibuprofen for topical delivery.

    abstract::The purpose of this study was to construct microemulsion-base hydrogel formulation for topical delivery of ibuprofen. Ethyl oleate (EO) was screened as the oil phase of microemulsions, due to a good solubilizing capacity of the microemulison systems and excellent skin permeation rate of ibuprofen. The pseudo-ternary p...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.02.015

    authors: Chen H,Chang X,Du D,Li J,Xu H,Yang X

    更新日期:2006-06-06 00:00:00

  • Entrapment and release of saquinavir using novel cationic solid lipid nanoparticles.

    abstract::Cationic solid lipid nanoparticles (CSLNs) with entrapped saquinavir (SQV) were fabricated by microemulsion method. Here, CSLNs were stabilized by polysorbate 80, and the lipid phase contained cationic stearylamine (SA) and dioctadecyldimethyl ammonium bromide (DODAB) and nonionic Compritol 888 ATO (CA) and cacao butt...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.08.050

    authors: Kuo YC,Chen HH

    更新日期:2009-01-05 00:00:00

  • Spray-freeze-drying production of thermally sensitive polymeric nanoparticle aggregates for inhaled drug delivery: effect of freeze-drying adjuvants.

    abstract::Inhalable dry-powder aggregates of drug-loaded thermally sensitive poly(caprolactone) (PCL) nanoparticles are produced using spray-freeze-drying (SFD) as the low melting point of PCL prohibits the use of high-temperature spray-drying. The effects of freeze-drying adjuvant formulation on the particle morphology, aerody...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.11.021

    authors: Cheow WS,Ng ML,Kho K,Hadinoto K

    更新日期:2011-02-14 00:00:00

  • Assessing the physical-chemical properties and stability of dapivirine-loaded polymeric nanoparticles.

    abstract::Nanocarriers may provide interesting delivery platforms for microbicide drugs and their characterization should be addressed early in development. Differently surface-engineered dapivirine-loaded, poly(epsilon-caprolactone) (PCL)-based nanoparticles (NPs) were obtained by nanoprecipitation using polyethylene oxide (PE...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.08.049

    authors: das Neves J,Amiji M,Bahia MF,Sarmento B

    更新日期:2013-11-18 00:00:00

  • Properties of polyethylene glycol 660 12-hydroxy stearate at a triglyceride/water interface.

    abstract::This study proposed a method to understand the surfactant role in the first step of the formulation of a novel generation of lipidic nanocapsules. A dynamic rheological protocol was applied using a pendant drop tensiometer in order to determine the interfacial properties of the initial mixture implied in the first for...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00144-8

    authors: Heurtault B,Saulnier P,Pech B,Proust JE,Benoît JP

    更新日期:2002-08-21 00:00:00

  • Modified local diatomite as potential functional drug carrier--A model study for diclofenac sodium.

    abstract::Diatomite makes a promising candidate for a drug carrier because of its high porosity, large surface area, modifiable surface chemistry and biocompatibility. Herein, refined diatomite from Kolubara coal basin, which complied with the pharmacopoeial requirements for heavy metals content and microbiological quality, was...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.10.047

    authors: Janićijević J,Krajišnik D,Čalija B,Vasiljević BN,Dobričić V,Daković A,Antonijević MD,Milić J

    更新日期:2015-12-30 00:00:00

  • Characterization of excipient enhanced growth (EEG) tobramycin dry powder aerosol formulations.

    abstract::Spray drying can be utilized to produce highly dispersible powder aerosol formulations. However, these formulations are known to be hygroscopic, leading to potential solid-state stability and aerosol performance issues. This study aims to investigate if control of the spray drying particle formation conditions could b...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.120027

    authors: Hassan A,Farkas D,Longest W,Hindle M

    更新日期:2020-12-15 00:00:00

  • Applications of NIR spectroscopy to monitoring and analyzing the solid state during industrial crystallization processes.

    abstract::Fiber-optic near infrared (NIR) spectroscopy was used to investigate several key features of the polymorphic transitions observed during the crystallization and the filtration of SaC, an Active Pharmaceutical Ingredient (API) produced by Sanofi-Synthelabo. Using few samples, the spectroscopic data were calibrated to p...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.01.003

    authors: Févotte G,Calas J,Puel F,Hoff C

    更新日期:2004-04-01 00:00:00